Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Beth Wilmot

Showing results (11-20 of 62) with videos related to

Pageof 7
Sort By:
Journal of Child Psychology and Psychiatry, and Allied Disciplines|August 26, 2015
Methylomic analysis of salivary DNA in childhood ADHD identifies altered DNA methylation in VIPR2Beth Wilmot, Rebecca Fry, Lisa Smeester, et al.
Translational Psychiatry|February 19, 2020
Large epigenome-wide association study of childhood ADHD identifies peripheral DNA methylation associated with disease and polygenic risk burdenMichael A Mooney, Peter Ryabinin, Beth Wilmot, et al.
The Journal of Rare Disorders|August 22, 2017
PHENOTYPIC VARIABILITY IN INDIVIDUALS WITH TYPE V OSTEOGENESIS IMPERFECTA WITH IDENTICAL IFITM5 MUTATIONSJamie Fitzgerald, Paul Holden, Hollis Wright, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 24, 2016
Pathway analysis in attention deficit hyperactivity disorder: An ensemble approachMichael A Mooney, Shannon K McWeeney, Stephen V Faraone, et al.
Alzheimer Disease and Associated Disorders|February 8, 2011
Microcephaly genes and risk of late-onset Alzheimer diseaseDeniz Erten-Lyons, Beth Wilmot, Pavana Anur, et al.
Endocrinology|December 1, 2011
A single-nucleotide polymorphism in the EAP1 gene is associated with amenorrhea/oligomenorrhea in nonhuman primatesAlejandro Lomniczi, Cecilia Garcia-Rudaz, Ranjani Ramakrishnan, et al.
Bioinformatics (Oxford, England)|January 11, 2013
HitWalker: variant prioritization for personalized functional cancer genomicsDaniel Bottomly, Beth Wilmot, Jeffrey W Tyner, et al.
BMC Genomics|February 6, 2015
Splicing landscape of the eight collaborative cross founder strainsChristina L Zheng, Beth Wilmot, Nicole Ar Walter, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 31, 2013
The genetics of gene expression in complex mouse crosses as a tool to study the molecular underpinnings of behavior traitsRobert Hitzemann, Daniel Bottomly, Ovidiu Iancu, et al.
Genome Medicine|November 30, 2013
Comparison of methods to identify aberrant expression patterns in individual patients: augmenting our toolkit for precision medicineDaniel Bottomly, Peter A Ryabinin, Jeffrey W Tyner, et al.
Pageof 7

Showing results (11-20 of 62) with videos related to

Sort By:
Pageof 7
Journal of Child Psychology and Psychiatry, and Allied Disciplines|August 26, 2015
Methylomic analysis of salivary DNA in childhood ADHD identifies altered DNA methylation in VIPR2Beth Wilmot, Rebecca Fry, Lisa Smeester, et al.
Translational Psychiatry|February 19, 2020
Large epigenome-wide association study of childhood ADHD identifies peripheral DNA methylation associated with disease and polygenic risk burdenMichael A Mooney, Peter Ryabinin, Beth Wilmot, et al.
The Journal of Rare Disorders|August 22, 2017
PHENOTYPIC VARIABILITY IN INDIVIDUALS WITH TYPE V OSTEOGENESIS IMPERFECTA WITH IDENTICAL IFITM5 MUTATIONSJamie Fitzgerald, Paul Holden, Hollis Wright, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 24, 2016
Pathway analysis in attention deficit hyperactivity disorder: An ensemble approachMichael A Mooney, Shannon K McWeeney, Stephen V Faraone, et al.
Alzheimer Disease and Associated Disorders|February 8, 2011
Microcephaly genes and risk of late-onset Alzheimer diseaseDeniz Erten-Lyons, Beth Wilmot, Pavana Anur, et al.
Endocrinology|December 1, 2011
A single-nucleotide polymorphism in the EAP1 gene is associated with amenorrhea/oligomenorrhea in nonhuman primatesAlejandro Lomniczi, Cecilia Garcia-Rudaz, Ranjani Ramakrishnan, et al.
Bioinformatics (Oxford, England)|January 11, 2013
HitWalker: variant prioritization for personalized functional cancer genomicsDaniel Bottomly, Beth Wilmot, Jeffrey W Tyner, et al.
BMC Genomics|February 6, 2015
Splicing landscape of the eight collaborative cross founder strainsChristina L Zheng, Beth Wilmot, Nicole Ar Walter, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 31, 2013
The genetics of gene expression in complex mouse crosses as a tool to study the molecular underpinnings of behavior traitsRobert Hitzemann, Daniel Bottomly, Ovidiu Iancu, et al.
Genome Medicine|November 30, 2013
Comparison of methods to identify aberrant expression patterns in individual patients: augmenting our toolkit for precision medicineDaniel Bottomly, Peter A Ryabinin, Jeffrey W Tyner, et al.
Pageof 7